Expert in Regulatory affairs & Compliance, she is well versed in strategic regulatory planning and due diligence in coordination of various activities involved in the development stage up to the life cycle of the product. Provided strategic and operational expertise (implementation of regulatory technical guidelines and new technology for submissions) to internal and client teams on regulatory and technical aspects of submissions to ensure timely and efficient handling of all-time bounded submissions. Devising and establishing company’s quality procedures and policies to meet GMP, GLP and GDP requirements. Assisted customers for global markets especially with USFDA, European union, Canada, Australia and Row markets.